Dipeptidyl Peptidase-4 Inhibitor (DPP4i) for the Control of Hyperglycemia in Patients With COVID-19

NCT ID: NCT04542213

Last Updated: 2021-03-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-08-01

Study Completion Date

2021-02-28

Brief Summary

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been a world health issue during the last months, affecting mostly countries with a high metabolic risk, like Mexico. Patients with type 2 diabetes (T2D) have an increased risk of any kind of infection as well as an increased mortality risk. Hyperglycemia has been established as an important predictor of mortality in patients with T2D and SARS-CoV-2. The standard treatment of hyperglycemia in hospitalized patients has been basen on insulin schemes, but recently evidence suggest the utility of some other drugs, reducing the risk of hypoglucemia and increasing the probability of a proper metabolic control. The goal of this study is to compare the utility of dipeptidyl peptidase-4 inhibitor (DPP4i) as a combination with insulin on metabolic control and prognosis in hospitalized patients with SARS-CoV-2 and hyperglycemia.

Detailed Description

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been a world health issue during the last months, affecting mostly countries with a high metabolic risk, like Mexico. Patients with type 2 diabetes (T2D) have an increased risk of any kind of infection as well as an increased mortality risk. Hyperglycemia has been established as an important predictor of mortality in patients with T2D and SARS-CoV-2. The standard treatment of hyperglycemia in hospitalized patients has been basen on insulin schemes, but recently evidence suggest the utility of some other drugs, reducing the risk of hypoglucemia and increasing the probability of a proper metabolic control. DPP4 enzyme has an ubiquitous distribution and has been considered as a pro-inflammatory enzyme, considering that DPP4 inhibitors could have and anti-inflammatory effect, as it has been shown in different works. The goal os this study is to compare the utility of DPP4 inhibitor as a combination with insulin on metabolic control and prognosis in hospitalized patients with SARS-CoV-2 and hyperglycemia. For this purpose we will randomize patients with SARS-CoV-2 and hyperglycemia to receive either the combination of DPP4i + insulin or insulin alone and will follow al algorithm treatment to define metabolic control as well as prognosis.

Conditions

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Hyperglycemia Covid19

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study will include two parallel groups of intervention
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors
Physicians who will be providing health support will not be aware of the treatment that patients will be receiving regarding this protocol, also the principal investigator and the personal who will be measuring glucose levels and prognosis, will not be aware of the group of treatment, since all the patients will be receiving the same protocol of insulin administration

Study Groups

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DPP4 inhibitor + insulin

Patients assigned to this group of treatment will receive Linagliptin 5mg orally once daily plus a basal-bolo insulin scheme

Group Type EXPERIMENTAL

Linagliptin tablet

Intervention Type DRUG

Linagliptin 5mg once daily plus a basal-bolus insulin scheme

Insulin scheme alone

Patients assigned to this group will receive only a basal-bolus insulin scheme

Group Type ACTIVE_COMPARATOR

Insulin

Intervention Type DRUG

Basal-bolus insulin scheme

Interventions

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Linagliptin tablet

Linagliptin 5mg once daily plus a basal-bolus insulin scheme

Intervention Type DRUG

Insulin

Basal-bolus insulin scheme

Intervention Type DRUG

Other Intervention Names

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Linagliptin Insulin group

Eligibility Criteria

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Inclusion Criteria

* Hospitalized patients with confirmed infection by SARS-CoV-2
* Hyperglycemia higher than 140 mg/dl
* Patients accepting oral medications
* Both sex
* Older than 18 years of age
* Patients who accept to participate in the study and sign the consent form

Exclusion Criteria

* Type 1 diabetes
* Pregnancy
* Hyperosmolar hyperglycemic state or diabetic ketoacidosis
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Regional de Alta Especialidad del Bajio

OTHER

Sponsor Role lead

Responsible Party

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Rodolfo Guardado Mendoza

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Rodolfo Guardado, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospital Regional de Alta Especialidad del Bajìo

Locations

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Hospital Regional de Alta Especialidad del Bajìo

Leòn, Guanajuato, Mexico

Site Status

Countries

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Mexico

References

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Document Type: Study Protocol and Statistical Analysis Plan

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CEI-22-2020

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Identifier Source: org_study_id

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